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FDA 510(k) Applications Submitted by ELENA JUGO
FDA 510(k) Number
Submission Date
Device Name
Applicant
K971646
05/05/1997
4F NYLEX ANGIOGRAPHY CATHETER/5F NYLEX ANGIOGRAPHY CATHETER
CORDIS CORP.
K001843
06/19/2000
S.M.A.R.T. NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
CORDIS CORP.
K152670
09/17/2015
DirectLink ICP Module, DirectLink ICP Extension Cable, Patient Monitor Interface Cables
Medos International SARL
K993646
10/29/1999
S.M.A.R.T. .018 NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
CORDIS CORP.
K994068
12/02/1999
S.M.A.R.T. NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
CORDIS CORP.
K970392
02/03/1997
CORDIS AVANTI+CATHETER SHEATH INTRODUCER SYSTEM
CORDIS CORP.
K970854
03/10/1997
5 FR AND 6 FR INFINITI ANGIOGRAPHIC CATHETER
CORDIS CORP.
K971608
05/01/1997
CORDIS BRITE TIP CATHETER SHEATH INTRODUCER SYSTEM
CORDIS CORP.
K041796
07/02/2004
PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
CORDIS CORPORATION
K003336
10/25/2000
MODIFICATION TO S.M.A.R.T NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
CORDIS CORP.
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